Metal-organic frameworks derived RuP2 with yolk-shell structure and efficient performance for hydrogen evolution reaction in both acidic and alkaline media

被引:47
|
作者
Luo, Jiahuan [1 ,2 ]
Wang, Jing [2 ]
Guo, Yao [2 ]
Zhu, Jiawei [1 ]
Jin, Huihui [1 ]
Zhang, Zhiwei [1 ]
Zhang, Daojun [3 ]
Niu, Yongsheng [2 ]
Hou, Shaogang [2 ]
Du, Jimin [3 ]
He, Daping [1 ]
Xiong, Yuli [4 ]
Chen, Lei [1 ]
Mu, Shichun [1 ,5 ]
Huang, Yunhui [6 ]
机构
[1] Wuhan Univ Technol, State Key Lab Adv Technol Mat Synth & Proc, Wuhan 430070, Peoples R China
[2] Anyang Inst Technol, Sch Chem & Environm Engn, Anyang 455000, Peoples R China
[3] Anyang Inst Technol, Coll Chem & Chem Engn, Anyang 455000, Peoples R China
[4] Wuhan Univ Technol, Sch Mat Sci & Engn, Wuhan 430070, Peoples R China
[5] Adv Energy Sci & Technol Guangdong Lab, Foshan Xianhu Lab, Xianhu Hydrogen Valley, Foshan 528200, Peoples R China
[6] Huazhong Univ Sci & Technol, Sch Mat Sci & Engn, State Key Lab Mat Proc & Die & Mould Technol, Wuhan 430074, Peoples R China
基金
中国国家自然科学基金;
关键词
Metal-organic frameworks; Ruthenium di-phosphide; DFT calculation; Hydrogen evolution reaction; Yolk-shell structure; UNIVERSAL SYNTHESIS STRATEGY; ELECTROCATALYSTS; CATALYSIS; SUPERIOR;
D O I
10.1016/j.apcatb.2021.121043
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Hydrogen generation from electrical water splitting has become a greatly increasing requirement for energy systems, however, highly effective and durable electrocatalysts towards universal-pH hydrogen evolution reaction (HER) remain a big challenge. Herein, we design and synthesize ruthenium di-phosphide (RuP2) confined in carbon layers (RuP2-C) with a unique yolk-shell structure (RuP2-C@RuP2-C) from MOF. As expected, it not only exceeds the HER activity of Pt catalysts, with very tiny overpotentials at 10 mA cm(-2) (9 and 17 mV in 1.0 M KOH and 0.5 M H2SO4, individually), but also has high stability. Besides, it also exhibits a low overpotential (40 mV) close to Pt catalysts and high stability in 1.0 M PBS, indicating that RuP2-C@RuP2-C (RPC@RPC) owns outstanding HER performance at all pH values. Density functional theory (DFT) calculation results further unravel that the P-site on the surface of RPC@RPC possesses low hydrogen adsorption energy, beneficial for boosting the HER activity.
引用
收藏
页数:8
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